一类新的非甾体类抗炎药预防和治疗眼部炎症。

G C Chiou, Q S Yao, M S Chang, T Okawara
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引用次数: 16

摘要

研究了新型非甾体抗炎药(NSAIAs)对晶状体蛋白、内毒素和白细胞介素-1诱导的眼部炎症的影响。结果发现,REV 5901、甲氧胺酸、吲哚美辛、CK-17、CK-102等大部分nsaid均能抑制晶状体蛋白诱导的炎症反应。内毒素通过释放IL-1间接诱导炎症,而IL-1可被少量药物抑制,包括CK-17、CK-102和强的松龙。而IL-1的直接作用只能被CK-17和强的松龙所抑制。因此,CK-17可能成为一种重要的NSAIA,其作用类似于皮质类固醇,但没有类固醇副作用。CK-17与大多数非甾体抗炎药不同,它对花生四烯酸代谢几乎没有影响。最重要的是,CK-17在抑制il -1诱导的葡萄膜炎方面的效力是强的松龙的2倍,而迄今为止测试的剂量没有发现副作用。
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Prevention and treatment of ocular inflammation with a new class of non-steroidal anti-inflammatory agents.

New non-steroidal anti-inflammatory agents (NSAIAs) were tested on lens protein-, endotoxin- and interleukin-1-induced ocular inflammation. It was found that most NSAIAs, including REV 5901, mefenamic acid, indomethacin, CK-17 and CK-102, inhibited lens protein-induced inflammation. Endotoxin induced inflammation indirectly through the release of IL-1 which was inhibited by fewer agents, including CK-17, CK-102 and prednisolone. However, the direct effect of IL-1 can only be suppressed by CK-17 and prednisolone. Therefore, CK-17 could become an important NSAIA which acts similarly to corticosteroids yet produces no steroidal side effects. CK-17 was different from most NSAIAs as it affected little, if any, arachidonate metabolism. Most importantly, CK-17 was found to be 2-fold more potent than prednisolone in inhibiting IL-1-induced uveitis, while no side effects were noted at doses tested to date.

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